NDC 60687-879-61
Divalproex Sodium 500 mg/1
Divalproex Sodium · TABLET, DELAYED RELEASE
Divalproex Sodium is a tablet, delayed release containing divalproex sodium at a strength of 500 mg/1. Manufactured by American Health Packaging.
Key Facts
- Brand Name
- Divalproex Sodium
- Generic Name
- Divalproex Sodium
- NDC Code (Package)
60687-879-61- NDC Code (Product)
60687-879- Manufacturer
- American Health Packaging
- Strength
- 500 mg/1
- Dosage Form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA079163
- Marketing Start
- 02/06/2025
Recall History
No Recall HistoryView Full Drug Page
Divalproex Sodium — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.